AD293 cell line人5型腺病毒转染人胚肾细胞株 BioVector NTCC质粒载体菌种细胞基因保藏中心
- 价 格:¥98965
- 货 号:AD293 cell line
- 产 地:北京
- BioVector NTCC典型培养物保藏中心
- 联系人:Dr.Xu, Biovector NTCC Inc.
电话:400-800-2947 工作微信:1843439339 (QQ同号)
邮件:Biovector@163.com
手机:18901268599
地址:北京
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AD293 cell line人5型腺病毒转染人胚肾细胞株
AD293 cell lineCat No.: NTCC690213The 293 Cell Line is a permanent line established from primary embryonic human kidney transformedwith human adenovirus type 5 DNA. The genes encoded by the E1 region of adenovirus (E1a and E1b)are expressed in these cells and participate in transactivation of viral promoters, allowing these cells toproduce high levels of protein. E1 also complements the E1-deletion in recombinant adenoviral vectors,allowing viral replication.BioVector's AD293 is derived from the parental 293 cell line, but specifically selected for adenovirus applications. Itoffers several advantages over the regular 293 cells:• Flattened morphology• Firm attachment to culture plate, ideal for amplification and tittering of adenovirus• Larger cell surface area resulting higher transfection and better yield of recombinant adenovirus. Medium1. Culture Medium: D-MEM (high glucose), 10% fetal bovine serum (FBS), 0.1 mM MEM NonEssentialAmino Acids (NEAA), 2 mM L-glutamine, 1% Pen-Strep (optional)2. Freeze Medium: 90% complete medium, 10% DMSOI. Establishing BioVector's AD293 Cultures from Frozen CellsMethods1. Place 10 mL of complete DMEM growth medium in a 50-mL conical tube. Thaw the frozencryovial of cells within 1–2 minutes by gentle agitation in a 37°C water bath. Decontaminate thecryovial by wiping the surface of the vial with 70% (v/v) ethanol.2. Transfer the thawed cell suspension to the conical tube containing 10 ml of growth medium.3. Collect the cells by centrifugation at 1000 rpm for 5 minutes at room temperature. Remove thegrowth medium by aspiration.4. Resuspend the cells in the conical tube in 15 mL of fresh growth medium by gently pipetting upand down.5. Transfer the 15 mL of cell suspension to a T-75 tissue culture flask. Place the cells in a 37°Cincubator at 5% CO2.6. Monitor cell density daily. Cells should be passaged when the culture reaches 95% confluence.D-MEM (high glucose), 10% fetal bovine serum (FBS), 0.1 mM MEM NonEssential Amino Acids (NEAA), 2 mM L-glutamine, 1% Pen-Strep (optional)
Supplier来源:BioVector NTCC Inc.
TEL电话:400-800-2947
Website网址: http://www.biovector.net
AD293 cell lineCat No.: NTCC690213The 293 Cell Line is a permanent line established from primary embryonic human kidney transformedwith human adenovirus type 5 DNA. The genes encoded by the E1 region of adenovirus (E1a and E1b)are expressed in these cells and participate in transactivation of viral promoters, allowing these cells toproduce high levels of protein. E1 also complements the E1-deletion in recombinant adenoviral vectors,allowing viral replication.BioVector's AD293 is derived from the parental 293 cell line, but specifically selected for adenovirus applications. Itoffers several advantages over the regular 293 cells:• Flattened morphology• Firm attachment to culture plate, ideal for amplification and tittering of adenovirus• Larger cell surface area resulting higher transfection and better yield of recombinant adenovirus. Medium1. Culture Medium: D-MEM (high glucose), 10% fetal bovine serum (FBS), 0.1 mM MEM NonEssentialAmino Acids (NEAA), 2 mM L-glutamine, 1% Pen-Strep (optional)2. Freeze Medium: 90% complete medium, 10% DMSOI. Establishing BioVector's AD293 Cultures from Frozen CellsMethods1. Place 10 mL of complete DMEM growth medium in a 50-mL conical tube. Thaw the frozencryovial of cells within 1–2 minutes by gentle agitation in a 37°C water bath. Decontaminate thecryovial by wiping the surface of the vial with 70% (v/v) ethanol.2. Transfer the thawed cell suspension to the conical tube containing 10 ml of growth medium.3. Collect the cells by centrifugation at 1000 rpm for 5 minutes at room temperature. Remove thegrowth medium by aspiration.4. Resuspend the cells in the conical tube in 15 mL of fresh growth medium by gently pipetting upand down.5. Transfer the 15 mL of cell suspension to a T-75 tissue culture flask. Place the cells in a 37°Cincubator at 5% CO2.6. Monitor cell density daily. Cells should be passaged when the culture reaches 95% confluence.D-MEM (high glucose), 10% fetal bovine serum (FBS), 0.1 mM MEM NonEssential Amino Acids (NEAA), 2 mM L-glutamine, 1% Pen-Strep (optional)
Supplier来源:BioVector NTCC Inc.
TEL电话:400-800-2947
Website网址: http://www.biovector.net
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